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Proplate

FDA UDI

Class II (US FDA UDI)

by Bioprotech Inc.

Identity

Trade Name
PROPLATE FDA UDI
Generic Name
Electrosurgical return electrode, single-use FDA UDI
Device Name
Disposable Solid Adult ESU Grouding Pad with Cable FDA UDI
Model / Reference
9571C (2 PCS) FDA UDI
Description
Disposable Solid Adult ESU Grouding Pad with Cable FDA UDI

Identifiers

Primary DI / UDI-DI
08809083944797 FDA UDI
510(k) Number
K073360 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical return electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical return electrode, single-use

Proplate by Bioprotech Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical return electrode, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioprotech Inc.

Sources (1)

  • FDA UDI 9a98a03c-933e-48e4-89b9-a013d5017e9b 35 fields · synced Jun 8, 2026